gentamicin sulfate

Generic: gentamicin sulfate

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gentamicin sulfate
Generic Name gentamicin sulfate
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

gentamicin sulfate 40 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1597
Product ID 51662-1597_0ff9b5b7-53ad-15f6-e063-6394a90a82aa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062420
Listing Expiration 2026-12-31
Marketing Start 2022-10-01

Pharmacologic Class

Classes
aminoglycoside antibacterial [epc] aminoglycosides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621597
Hyphenated Format 51662-1597

Supplemental Identifiers

RxCUI
1870650
UNII
8X7386QRLV

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name gentamicin sulfate (source: ndc)
Generic Name gentamicin sulfate (source: ndc)
Application Number ANDA062420 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/mL
source: ndc
Packaging
  • 25 POUCH in 1 CASE (51662-1597-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1597-2) / 2 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

Ingredients (1)

gentamicin sulfate (40 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "0ff9b5b7-53ad-15f6-e063-6394a90a82aa", "openfda": {"unii": ["8X7386QRLV"], "rxcui": ["1870650"], "spl_set_id": ["e9fbe619-2afe-f1d7-e053-2a95a90aab29"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "25 POUCH in 1 CASE (51662-1597-3)  / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1597-2)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51662-1597-3", "marketing_start_date": "20221001"}], "brand_name": "GENTAMICIN SULFATE", "product_id": "51662-1597_0ff9b5b7-53ad-15f6-e063-6394a90a82aa", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]"], "product_ndc": "51662-1597", "generic_name": "GENTAMICIN SULFATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GENTAMICIN SULFATE", "active_ingredients": [{"name": "GENTAMICIN SULFATE", "strength": "40 mg/mL"}], "application_number": "ANDA062420", "marketing_category": "ANDA", "marketing_start_date": "20221001", "listing_expiration_date": "20261231"}